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Data / Medical devices / Oxyhemoglobin

Oxyhemoglobin (GGZ): 3 FDA-registered makers in 2 countries

3 establishments in 2 countries are registered with the FDA to make Oxyhemoglobin (product code GGZ, Class 2, 21 CFR 864.7500). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on April 6, 2020, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code
GGZ
Device class
2
Regulation
864.7500
Medical specialty
Hematology

Makers by country

CountryMakers
United States2
Switzerland1

Makers of Oxyhemoglobin

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Nova Biomedical CorporationWaltham, MA, United StatesManufacturer, Manufacturer for export, Remanufacturer1August 23, 2018000api.fda.gov
Nova Biomedical CorporationBillerica, MA, United StatesManufacturer, Manufacturer for export, Remanufacturer1August 23, 2018000api.fda.gov
Roche Diagnostics International Ltd.ROTKREUZ Zug, SwitzerlandManufacturer0000api.fda.gov

Updated April 6, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.